Canonical Allele Identifier:
CA13492252
Community Standard Title: NC_000011.10:g.112164784A>C
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.112164784A>C , CM000673.2:g.112164784A>C | GRCh38 |
| NC_000011.9:g.112035507A>C , CM000673.1:g.112035507A>C | GRCh37 |
| NC_000011.8:g.111540717A>C | NCBI36 |
| NG_028143.1:g.4334T>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| ENST00000525987.5:n.320-5635A>C | |
| ENST00000531744.5:c.315-5635A>C | ENSP00000456957.1:n.315-5635A>C |
| ENST00000532699.1:c.315-5635A>C | ENSP00000456434.1:n.315-5635A>C |